NACSOC-02: Camrelizumab Combined With Neoadjuvant Chemotherapy After Stent Placement for Left-Sided Obstructive Colonic Cancer

Sponsor
Beijing Chao Yang Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT05202314
Collaborator
(none)
20
1
1
60.6
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Study Details

Study Description

Brief Summary

Patients with obstruction are associated with worse oncologic outcomes compared with those having nonobstructive tumors. Conventionally, patients with malignant large bowel obstruction receive emergency surgery, with morbidity rates of 30%-60% and mortality rates of 7-22%, and about two-thirds of such patients end up with a permanent stoma. Self-expanding metallic stents (SEMS) haven been used as a bridge to surgery (to relieve obstruction prior to elective surgery) in patients with potentially resectable colorectal cancer. Several clinical trials demonstrate that SEMS as a bridge to surgery may be superior to emergency surgery considering the short-term outcomes. SEMS is associated with lower morbidity and mortality rate, increased primary anastomosis rate, and decreased stoma creation rate. Although about half of patients can achieve primary anastomosis after stent placement, the primary anastomosis rate is still significantly lower compared with nonobstructing elective surgery. The interval between stent placement and surgery may be not long enough that bowel decompression is insufficient at the time of operation. Furthermore#the long-term oncologic results regarding SEMS as a bridge to surgery are still limited and contradictory. Sabbagh et al. suggest worse overall survival of patients with SEMS insertion compared with emergency surgery, the 5-year cancer-specific mortality was significantly higher in the SEMS group (48% vs 21%, respectively, P=0.02). One interpretation is that tumor cells may disseminate during the procedure of colonic stenting placement. Immunotherapy has proven to be highly effective as first-line treatment of metastatic colorectal cancer (CRC). And immunotherapy also has emerged as a neoadjuvant approach, possibly changing treatment strategy for both primary resectable and metastatic CRC. We hypothesis that, regardless of the MSI state, immunotherapy (Camrelizumab, an anti-PD-1 antibody) combined with chemotherapy after stenting may improve overall survival by eradicating micrometastasis. Moreover, immunotherapy (Camrelizumab, an anti-PD-1 antibody) combined with neoadjuvant chemotherapy prolongs the interval between stent placement and surgery, and the time for bowel decompression is more sufficient, which may increase the success rate of primary anastomosis and decrease risk of stoma formation, and furthermore, improve OS and PFS.

Condition or Disease Intervention/Treatment Phase
  • Drug: Immunotherapy (Camrelizumab)
N/A

Detailed Description

We hypothesis that, regardless of the MSI state, immunotherapy combined with immediate chemotherapy after stenting may improve overall survival by eradicating micrometastasis. Moreover, immunotherapy (Camrelizumab, an anti-PD-1 antibody) combined with neoadjuvant chemotherapy prolongs the interval between stent placement and surgery, and the time for bowel decompression is more sufficient, which may increase the success rate of primary anastomosis and decrease risk of stoma formation, and furthermore, improve OS and PFS.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
20 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Camrelizumab Combined With Neoadjuvant Chemotherapy After Stent Placement Versus Surgery Alone for Left-Sided Obstructive Colonic Cancer
Actual Study Start Date :
Dec 12, 2021
Anticipated Primary Completion Date :
Dec 30, 2023
Anticipated Study Completion Date :
Dec 30, 2026

Arms and Interventions

Arm Intervention/Treatment
Experimental: Immunotherapy group

After clinical success of colonic stenting, regardless of the MSI state all patients will receive Immunotherapy (Camrelizumab 200mg) for 2 cycles compined with neoadjuvant chemotherapy with mFOLFOX6 regimen for 3 cycles or CapeOx regimen for 2 cycles. Patients will undergo surgery 2-3 weeks after the last cycle of chemotherapy, type and extent of the surgery will be selected by the surgeon.

Drug: Immunotherapy (Camrelizumab)
After clinical success of colonic stenting, regardless of the MSI state, patients will receive Immunotherapy (Camrelizumab 200mg) for 2 cycles compined with neoadjuvant chemotherapy with mFOLFOX6 regimen for 3 cycles or CapeOx regimen for 2 cycles. Patients will undergo surgery 2-3 weeks after the last cycle chemotherapy
Other Names:
  • Chemotheray (CAPOX or mFOLFOX6)
  • Outcome Measures

    Primary Outcome Measures

    1. Pathological complete remission [2 weeks after patients received radical operation]

      No tumor cell found in surgical specimens

    Secondary Outcome Measures

    1. Disease Free Survival [3 years after operation]

      No tumor regrowth or recurrence or metastasis found

    2. Overall Survival [3 years after operation]

      Survive during following

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Radiologically proven colonic obstruction of the left colon/upper rectum presumed secondary to a carcinoma

    • Able to give written, informed consent

    • Primary tumor was resectable

    • ECOG score 0 or 1

    • Haemoglobin greater than 100 g/L after transfusion before chemotherapy,

    • White blood cells greater than 3.0×10# /L

    • Platelets greater than 100×10# / L;

    • Glomerular filtration rate greater than 50 mL per minute as calculated by the Wright or Cockroft formula

    • Bilirubin less than 1.5×Upper Limit of Normal(ULN)

    • ALT and AST less than 2.5×ULN

    Exclusion Criteria:
    • Distal rectal cancers(equal or less than 10cm from the anal verge)

    • Patients with signs of peritonitis and/or bowel perforation

    • Patients who did not give informed consent

    • Patients who were considered unfit for operative treatment or refuse surgery.

    • Patients with suspected or proven metastatic adenocarcinoma;

    • Patients with unresectable colorectal cancer, or planning for palliative treatment.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Beijing Chaoyang Hospital, Capital Medical University Beijing Beijing China 100020

    Sponsors and Collaborators

    • Beijing Chao Yang Hospital

    Investigators

    • Principal Investigator: Zhen Jun Wang, MD, Beijing Chao Yang Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Zhen Jun Wang, Professor, Beijing Chao Yang Hospital
    ClinicalTrials.gov Identifier:
    NCT05202314
    Other Study ID Numbers:
    • 2021-12-24
    First Posted:
    Jan 21, 2022
    Last Update Posted:
    Jan 21, 2022
    Last Verified:
    Jan 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 21, 2022